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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Benzothiazolamine, dichloro-

Nc1sc2c(n1)c(Cl)c(cc2)Cl Request for Quotation
Chemical Name: 2-Benzothiazolamine, dichloro-
CAS Number: 1849-71-4
Product Number: AG00ACUW(AGN-PC-0JUNYD)
Synonyms:
MDL No:
Molecular Formula: C7H4Cl2N2S
Molecular Weight: 219.0911

Identification/Properties

Computed Properties
Molecular Weight:
219.083g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
217.947g/mol
Monoisotopic Mass:
217.947g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
181
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,5-Dichlorobenzo[d]thiazol-2-amine is a versatile compound widely used in chemical synthesis as a key building block. Its unique structure allows for the incorporation of both benzothiazole and amine functional groups, making it valuable in the creation of diverse chemical compounds.One common application of 4,5-Dichlorobenzo[d]thiazol-2-amine is in the synthesis of pharmaceuticals. The presence of the amine group enables the compound to participate in various organic reactions such as reductive amination, nucleophilic substitution, and amide formation. This makes it suitable for the preparation of drug candidates and intermediates in the pharmaceutical industry.Moreover, the benzothiazole moiety in 4,5-Dichlorobenzo[d]thiazol-2-amine imparts unique properties that can be utilized in the development of agrochemicals, dyes, and materials. By incorporating this compound into molecular structures, chemists can modulate the chemical and physical characteristics of the final products, leading to a wide range of applications.Overall, the synthesis of 4,5-Dichlorobenzo[d]thiazol-2-amine plays a crucial role in the creation of novel chemical entities with potential applications across various industries. Its versatile nature and reactivity make it a valuable tool for chemists seeking to design and produce compounds with tailored properties and functionalities.